Control of echolocation pulses by neurons of the nucleus ambiguus in the rufous horseshoe bat,Rhinolophus rouxi

Horseradish peroxidase was applied by inotophoretic injections to physiologically identified regions of the laryngeal motor nucleus, the nucleus ambiguus in the CF/FM bat Rhinolophus rouxi. The connections of the nucleus ambiguus were analysed with regards to their possible functional significance in the vocal control system, in the respiration control system, and in mediating information from the central auditory system. The nucleus ambiguus is reciprocally interconnected with nuclei involved in the generation of the vocal motor pattern, i.e., the homonomous contralateral nucleus and the area of the lateral reticular formation. Similarly, reciprocal connections are found with the nuclei controlling the rhythm of respiration, i.e., medial parts of the medulla oblongata and the parabrachial nuclei. Afferents to the nucleus ambiguus derive from nuclei of the 'descending vocalization system' (periaqueductal gray and cuneiform nuclei) and from motor control centers (red nucleus and frontal cortex). Afferents to the nucleus ambiguus, possibly mediating auditory influence to the motor control of vocalization, come from the superior colliculus and from the pontine nuclei. The efferents from the pontine nuclei are restricted to rostral parts of the nucleus ambiguus, which hosts the motoneurons of the cricothyroid muscle controlling the call frequency.     

Interferon induction by platinum(II)-poly(I).poly(C) complexes

The effect of the interaction between poly(I).poly(C) and cis-dichloro-diammineplatinum(II) (cis-Pt), its trans analogue and chloro-diethylene-triamminoplatinum(II) (dien-Pt) on interferon induction activity was investigated. The covalent monodentate fixation of the three compounds on N7 of inosine has different effects on the structure and thermostability of poly(I). poly(C) which is well reflected by the interferon induction activity of the samples. Thus, the sandwich stabilization by dien-Pt at low binding ratios is manifested by an increased interferon induction and a high resistance towards RNAase degradation. The destabilization of the duplex by cis-Pt decreases interferon induction, accompanied by an increase in RNAase sensitivity of the complexes. In the case of trans-Pt the duplex structure is little perturbed and interferon induction is essentially maintained.     

Further characterization of cooperative interactions of monoclonal antibodies

We reported previously that mixtures of some monoclonal antibodies directed against the glycoprotein hormone human chorionic gonadotropin (hCG) had a higher affinity for the antigen than either monoclonal antibody separately. The synergistic interaction could no longer be detected when one of the antibodies was replaced with its F(ab) fragment. This cooperative interaction has now been further characterized. One-half of 10 possible pairs prepared from five IgG1 monoclonal antibodies against hCG result in a synergistic interaction. The addition of an IgG2b monoclonal antibody to one of the IgG1 monoclonal antibodies also induces a cooperative interaction, which shows that the effect is not subclass restricted. Cooperative interactions between antibodies are also not restricted to solution conditions; adsorption of one antibody to a solid support appears to increase the cooperative effect. Indeed, one pair of antibodies that failed to bind hCG synergistically in solution did so when one antibody was bound to a solid surface. The liquid phase antibody also has an effect on the specificity of the solid phase antibody. The sensitivity of the solid phase assay system has enabled us to develop a rapid method of determining if two monoclonal antibodies can bind to an antigen simultaneously. A quantitative theoretical model has been devised that successfully predicts the cooperative behavior observed between antibodies and should be useful in devising conditions that result in sensitive solid phase radioimmunoassays.     

Ligation of highly modified bacteriophage DNA

After digestion by TaqI or nicking by DNAase I, five highly modified bacteriophage DNAs were tested as substrates for T4 DNA ligase. The DNAs used were from phages T4, XP12, PBS1, SP82, and SP15, which contain as a major base either glucosylated 5-hydroxymethylcytosine, 5-methylcytosine, uracil, 5-hydroxymethyluracil, or phosphoglucuronated, glucosylated 5-(4′,5′-dihydroxypentyl)uracil, respectively. The relative ability of cohesive-ended TaqI fragments of these DNAs and of normal, λ DNA to be ligated was as follows: $\text{λ}\text{DNA}\text{=}\text{XP}\text{12}\text{DNA}\text{>}\text{SP}\text{82}\text{DNA}\text{?}\text{nonglucosylated}\text{T}\text{4}\text{DNA}\text{>}\text{T}\text{4}\text{DNA}\text{=}\text{PBS}\text{1}\text{DNA}\text{?}\text{SP}\text{15}\text{DNA}$. TaqI-T4 DNA fragments were also inefficiently ligated by Escherichia coli DNA ligase. However, annealing-independent ligation of DNAase I-nicked T4, PBS1, and λ DNAs was equally efficient. We conclude that the poor ligation of TaqI fragments of T4 and PBS1 DNAs was due to the hydroxymethylation (and glucosylation) of cytosine residues at T4's cohesive ends and the substitution of uracil residues for thymine residues adjacent to PBS1's cohesive ends destabilizing the annealing of the restriction fragments. Only SP15 DNA with its negatively charged, modified base was unable to serve as a substrate for T4 DNA ligase in an annealing-independent reaction; therefore, its modification directly interfered with enzyme binding or catalysis.     

Zur Wirkung des Lichtes auf die circadiane Periodik des Stoffwechsels und der Aktivität beim Buchfinken (Fringilla coelebs L.)

Zusammenfassung Bei 8 Buchfinken (4, 4) wurden Sauerstoffverbrauch und Hüpfaktivitätsowohl unter Bedingungen eines künstlichen Licht-Dunkel-Wechsels (LD 1212 Std; ohne Dämmerung) als auch im Dauerlicht (LL) bei konstanter Umgebungstemperatur (18–20° C) kontinuierlich gemessen. Im 1. Teil des Versuchs wurde die Beleuchtungsstärke während der Dunkelzeit (D) zwischen 0,01 und 1,0 Lux bei gleichbleibender Beleuchtungsstärke während der Lichtzeit (10 Lux) geändert. Im 2. Teil des Versuchs wurden die Vögel im Dauerlicht von 1 und 10 Lux untersucht. Vier Vögel wurden zusätzlich bei 100 Lux gemessen.Das mittlere Niveau des Sauerstoffverbrauchs (pro Std) und die mittlere Aktivitätsmenge (pro Stunde) während einer Periode sind bei der Mehrzahl der untersuchten Vögel linear und positiv miteinander korreliert (Abb. 2 und 3; Tabelle 1).Änderungen des mittleren Aktivitätsumsatzes (Differenz von mittlerem Niveau des Gesamtumsatzes und des Ruheumsatzes) sind ebenfalls positiv mit Änderungen der Aktivitätsmenge korreliert. Diese Aussage beruht auf der Voraussetzung, daß sich die circadiane Periodik des Gesamtstoffwechsels aus mindestens zwei Periodizitäten zusammensetzt: der Periodik des Grundstoffwechsels (vegetative Periodik) und der Periodik von Ruhe und Aktivität (Aktivitätsperiodik).Bei Änderungen des Zeitgebers (Erniedrigung der Zeitgeberamplitude und gleichzeitige Erhöhung der mittleren Beleuchtungsstärke) werden folgende Parameter signifikant verändert: die positive Phasenwinkel-Differenz zwischen Stoffwechselperiodik und Zeitgeber wird vergrößert, die Dauer der Aktivität (Aktivitätsumsatz ₃ ) wird verlängert, die Schwingungsbreite der Stoffwechselperiodik wird erniedrigt (Abb. 4; Tabelle 2).Unter Dauerlicht-Bedingungen werden durch eine Erhöhung der Beleuchtungsstärke von 1 auf 10 Lux folgende circadianen Parameter erhöht: die Frequenz, das mittlere Niveau der Stoffwechselperiodik (Gleichwert), der Ruheumsatz, das -Verhältnis (Verhältnis Aktivitätszeit/Ruhezeit) und die Aktivitätsmenge pro Zeiteinheit. Die Schwingungsbreite der Stoffwechselperiodik bleibt unverändert (Abb. 5). Außerdem besteht eine regelhafte Beziehung zwischen dem Formfaktor der Stoffwechselschwingung und der Beleuchtungsstärke, beziehungsweise der Spontanfrequenz. Erhöhung der Beleuchtungsstärke von 10 auf 100 Lux hat unterschiedliche Wirkungen auf die circadianen Parameter der 4 gemessenen Vögel.Die unter Dauerlicht-Bedingungen gewonnenen Ergebnisse folgen der modifizierten circadianen Regel, die eine positive Korrelation zwischen Frequenz und Gleichwert der autonomen circadianen Schwingung fordert (Abb. 7).Die unter Zeitgeber-Bedingungen (Licht-Dunkel-Wechsel) gewonnenen Ergebnisse werden auf der Grundlage einer vorwiegenden Beeinflussung des circadianen Schwingers durch die Amplitude der Zeitgeber-Periodik (Zeitgeberstärke) gedeutet. Änderungen der Beleuchtungsstärke während der Dunkelzeit (im Bereich der gebotenen Lichtintensitäten) haben keinen regelhaften Einfluß auf die Stoffwechselparameter der Periodik.

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On the effect of light upon the crcadian rhythms of metabolism and activity in the chaffinch (Fringilla coelebs L.)

Summary Oxygen consumption and hopping activity of 8 chaffinches (4 males, 4 females) were measured simultaneously (I) in an artificial 1212 hr light-dark-cycle (LD; without twilight) and (II) in continuous illumination, both at constant temperature (18–20°C). During the first part of the experiment illumination during darktime (D) was varied in both directions between 0.01 and 1.0 lux. Light intensity in L (lighttime) remained constant (10 lux). In the second part of the experiment the birds were exposed to a continuous illumination of 1 and 10 lux. Four birds were also measured at 100 lux.For the majority of the birds, the mean level of oxygen consumption per hour and the average amount of activity (contacts per hour) during one circadian period are positively and linearly correlated to each other (Fig. 2 and 3; Table 1).Changes in the level of the activity metabolism — i.e. the difference between mean level of total metabolism and resting metabolism — are also positively correlated to changes in the amount of activity. This statement is based on the assumption that there exist at least 2 rhythms as basic components of the circadian rhythm of total metabolism: the rhythm of basal metabolic rate (BMR) or vegetative rhythm and the rhythm of activity and rest (activity rhythm).By variation of the Zeitgeber — simultaneous decrease in amplitude and increase in mean level of light intensity — the following parameters are significantly changed: the phase-angle difference between the circadian rhythm of metabolism and the Zeitgeber is increased (positive phase-angle differences are changed in positive direction), the activity time is lengthened, and the amplitude of the rhythm (range of oscillation) is diminished (Fig. 4; Table 2).With an increase in light intensity from 1 to 10 lux (continuous illumination), the following parameters are increased: the frequency of the rhythm, the mean level of metabolism per period, the resting metabolic rate, the -ratio (i.e. ratio activity time/rest time), and the total amount of activity per unit time. The range of oscillation remains unchanged (Fig. 5). There is also a regular change of the form-factor characterizing the shape of the metabolic oscillation, which depends upon light intensity as well as upon frequency (Fig. 8). Increasing light intensity from 10 to 100 lux affected differently the circadian parameters of the four birds tested.The results obtained in continuous illumination follow the modified circadian rule which postulates the positive correlation between frequency and mean level of the autonomous circadian oscillation (Fig. 7).The results obtained under the influence of a Zeitgeber (light-dark-cycle) are interpreted on the basis of the primary influence of the Zeitgeber amplitude (strength of the Zeitgeber) upon the circadian oscillation. The given changes in light intensity during darktime have no significant effect on the metabolic parameters of the rhythm.

     

Bacteriology of manganese nodules: III. Reduction of MnO(2) by two strains of nodule bacteria

MnO₂ reduction by aerobic growing cultures of Bacillus 29 and coccus 32, isolated from ferromanganese nodules, was assessed for 7 days. A 1-day lag was observed before the onset of MnO₂ reduction by either culture. Addition of HgCl₂ to a final concentration of about 10^-3 M caused a rapid cessation of MnO₂ reduction by the growing cultures. Neither culture reduced MnO₂ when grown under continued anaerobiosis from the start of an experiment. However, if conditions were made anaerobic after MnO₂ reduction was initiated, reduction continued at a rate only slightly lower than that under aerobic conditions. Resting-cell cultures reduced MnO₂ equally well aerobically and anaerobically, provided that ferricyanide was present to serve as electron carrier. These findings showed that oxygen is needed for culture adaptation to MnO₂ reduction, and that oxygen does not interfere with microbial MnO₂ reduction itself. Both cultures caused sharp drops in the pH of the medium during MnO₂ reduction: with coccus 32, during the entire incubation time; with Bacillus 29, for the first 3 days. The E_h of the medium fluctuated with either culture and never fell below 469 mv with Bacillus 29 and below 394 mv with coccus 32. The rates of glucose consumption and Mn²⁺ release by Bacillus 29 and coccus 32 were fairly constant, but the rates of lactate and pyruvate production were not. Although acid production undoubtedly helped in the reduction of pyrolusite (MnO₂) by the bacteria, it did not appear to be important in the reduction of manganese oxide in ferromanganese nodules, as shown by the results with a nodule enrichment.     

Bacteriology of Manganese Nodules: III. Reduction of MnO2 by Two Strains of Nodule Bacteria1

MnO₂ reduction by aerobic growing cultures of Bacillus 29 and coccus 32, isolated from ferromanganese nodules, was assessed for 7 days. A 1-day lag was observed before the onset of MnO₂ reduction by either culture. Addition of HgCl₂ to a final concentration of about 10^-3 M caused a rapid cessation of MnO₂ reduction by the growing cultures. Neither culture reduced MnO₂ when grown under continued anaerobiosis from the start of an experiment. However, if conditions were made anaerobic after MnO₂ reduction was initiated, reduction continued at a rate only slightly lower than that under aerobic conditions. Resting-cell cultures reduced MnO₂ equally well aerobically and anaerobically, provided that ferricyanide was present to serve as electron carrier. These findings showed that oxygen is needed for culture adaptation to MnO₂ reduction, and that oxygen does not interfere with microbial MnO₂ reduction itself. Both cultures caused sharp drops in the pH of the medium during MnO₂ reduction: with coccus 32, during the entire incubation time; with Bacillus 29, for the first 3 days. The E_h of the medium fluctuated with either culture and never fell below 469 mv with Bacillus 29 and below 394 mv with coccus 32. The rates of glucose consumption and Mn²⁺ release by Bacillus 29 and coccus 32 were fairly constant, but the rates of lactate and pyruvate production were not. Although acid production undoubtedly helped in the reduction of pyrolusite (MnO₂) by the bacteria, it did not appear to be important in the reduction of manganese oxide in ferromanganese nodules, as shown by the results with a nodule enrichment.